chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44968927	44968928	A	G	45	GENIC	homozygous	110692997
2	44968936	44968937	T	C	46	GENIC	homozygous	110930229
2	44968937	44968938	G	C	46	GENIC	homozygous	110930230
2	44968939	44968940	C	T	46	GENIC	homozygous	110930231
2	44969058	44969059	G	A	39	GENIC	homozygous	110692999
2	44969082	44969083	A	C	37	GENIC	homozygous	110508379
2	44969170	44969171	G	C	41	GENIC	homozygous	110693001
2	44969206	44969206		GATT	40	GENIC	homozygous	130862144
2	44969246	44969247	C		32	GENIC	heterozygous	130862145
2	44969457	44969458	G	A	44	GENIC	homozygous	110693003
2	44971349	44971350	A		24	GENIC	possibly homozygous	130862148
2	44972666	44972667	T	C	29	GENIC	homozygous	120167404
2	44972834	44972835	C	A	60	GENIC	homozygous	110508386
2	44973278	44973279	C	A	15	GENIC	homozygous	110508387
2	44973901	44973902	C	T	28	GENIC	homozygous	110508389
2	44974051	44974052	C	T	37	GENIC	homozygous	110508390
2	44974458	44974459	A	G	38	GENIC	homozygous	110508391
2	44974473	44974474	A	G	31	GENIC	homozygous	110508392
2	44979807	44979808	C	T	36	GENIC	heterozygous	109725794
2	44970583	44970583		CAAGCAAGCAAG	25	GENIC	homozygous	131599791
2	44976090	44976096	GTGTGT		34	GENIC	homozygous	131599792
2	44979737	44979738	A	G	49	GENIC	heterozygous	109725787
2	44979738	44979739	A	G	49	GENIC	heterozygous	109725789
2	44979768	44979769	G	A	48	GENIC	heterozygous	109725791
2	44977179	44977180	C	T	41	GENIC	homozygous	120189584
2	44979120	44979121	T	C	25	GENIC	homozygous	131608639
2	44980105	44980106	A		26	GENIC	homozygous	131599793
2	44980715	44980716	A	G	44	GENIC	homozygous	120167405